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The chemical compound "(3aR,4aS,8aR,9aR)-3-[1-Benzenesulfinyl-meth-(E)-ylidene]-8a-methyl-5-methylene-decahydro-naphtho[2,3-b]furan-2-one" is a complex, chiral molecule with a unique structure. It features de acahydro-naphtho[2,3-b]furan-2-one core, which is a type of polycyclic aromatic compound with a furan ring fused to a decahydro-naphtho system. The molecule is characterized by its specific stereochemistry, with four chiral centers at positions 3a, 4a, 8a, and 9a, each having a specific configuration (R or S). A key functional group in (3aR,4aS,8aR,9aR)-3-[1-Benzenesulfinyl-meth-(E)-ylidene]-8a-methyl-5-methylene-decahydro-naphtho[2,3-b]furan-2-one is the 1-benzenesulfinyl-meth-(E)-ylidene moiety, which is a sulfur-containing group that contributes to the molecule's reactivity and properties. The 8a-methyl and 5-methylene groups further modify the structure, influencing its physical and chemical characteristics. (3aR,4aS,8aR,9aR)-3-[1-Benzenesulfinyl-meth-(E)-ylidene]-8a-methyl-5-methylene-decahydro-naphtho[2,3-b]furan-2-one is likely to be of interest in organic chemistry due to its potential applications in the synthesis of pharmaceuticals or other specialty chemicals, given its structure intricate and the presence of multiple functional groups.

76886-51-6

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76886-51-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76886-51-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,8 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76886-51:
(7*7)+(6*6)+(5*8)+(4*8)+(3*6)+(2*5)+(1*1)=186
186 % 10 = 6
So 76886-51-6 is a valid CAS Registry Number.

76886-51-6Relevant academic research and scientific papers

Synthesis of Deuterium-Labeled Sesquiterpene Lactones Isolated from Inula helenium L.

Schaeffer, Marcel,Stampf, Jean-Luc,Benezra, Claude

, p. 6106 - 6113 (2007/10/02)

Reduction of the vinyl sulfoxides 9 and 10 derived from isoalantolactone (1) and alantolactone (2) with NaBD4 yielded deuterium-labeled lactones 11 and 12.Amalgam reduction of sulfides 7 and 8 or sulfoxides 9 and 10 gave labeled products but not the expected deuterated lactones 11 and 12.Satisfactory deuteration of alantolactone 2 could be achieved by CF3COOD hydrolysis of (tributylstannyl)alantolactone (23) obtained in four steps from alantolactone 2.

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